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Developing a Canadian Real-World Evidence Action Plan across the Drug Life Cycle

Policy makers face challenges with the number of drugs for rare indications and rapidly rising costs. In facing these challenges, decision-makers see real-world evidence (RWE) as an opportunity. Health Canada and the Canadian Agency for Drugs and Technologies in Health (CADTH) recently announced the...

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Detalles Bibliográficos
Autores principales: Tadrous, Mina, Ahuja, Tarry, Ghosh, Basanti, Kropp, Rhonda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Longwoods Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294449/
https://www.ncbi.nlm.nih.gov/pubmed/32538348
http://dx.doi.org/10.12927/hcpol.2020.26225
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author Tadrous, Mina
Ahuja, Tarry
Ghosh, Basanti
Kropp, Rhonda
author_facet Tadrous, Mina
Ahuja, Tarry
Ghosh, Basanti
Kropp, Rhonda
author_sort Tadrous, Mina
collection PubMed
description Policy makers face challenges with the number of drugs for rare indications and rapidly rising costs. In facing these challenges, decision-makers see real-world evidence (RWE) as an opportunity. Health Canada and the Canadian Agency for Drugs and Technologies in Health (CADTH) recently announced their intent to co-develop an action plan to optimize the process for the systematic use and integration of RWE into both regulatory and reimbursement decision-making in Canada. When implemented, this will have a significant impact on how drugs are approved and paid for in Canada. We highlight the key opportunities, barriers and future directions related to the use of RWE throughout the life cycle of drugs in Canada.
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spelling pubmed-72944492020-06-18 Developing a Canadian Real-World Evidence Action Plan across the Drug Life Cycle Tadrous, Mina Ahuja, Tarry Ghosh, Basanti Kropp, Rhonda Healthc Policy Research Paper Policy makers face challenges with the number of drugs for rare indications and rapidly rising costs. In facing these challenges, decision-makers see real-world evidence (RWE) as an opportunity. Health Canada and the Canadian Agency for Drugs and Technologies in Health (CADTH) recently announced their intent to co-develop an action plan to optimize the process for the systematic use and integration of RWE into both regulatory and reimbursement decision-making in Canada. When implemented, this will have a significant impact on how drugs are approved and paid for in Canada. We highlight the key opportunities, barriers and future directions related to the use of RWE throughout the life cycle of drugs in Canada. Longwoods Publishing 2020-05 /pmc/articles/PMC7294449/ /pubmed/32538348 http://dx.doi.org/10.12927/hcpol.2020.26225 Text en Copyright © 2020 Longwoods Publishing http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial 4.0 License, which permits rights to copy and redistribute the work for non-commercial purposes only, provided the original work is given proper attribution.
spellingShingle Research Paper
Tadrous, Mina
Ahuja, Tarry
Ghosh, Basanti
Kropp, Rhonda
Developing a Canadian Real-World Evidence Action Plan across the Drug Life Cycle
title Developing a Canadian Real-World Evidence Action Plan across the Drug Life Cycle
title_full Developing a Canadian Real-World Evidence Action Plan across the Drug Life Cycle
title_fullStr Developing a Canadian Real-World Evidence Action Plan across the Drug Life Cycle
title_full_unstemmed Developing a Canadian Real-World Evidence Action Plan across the Drug Life Cycle
title_short Developing a Canadian Real-World Evidence Action Plan across the Drug Life Cycle
title_sort developing a canadian real-world evidence action plan across the drug life cycle
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294449/
https://www.ncbi.nlm.nih.gov/pubmed/32538348
http://dx.doi.org/10.12927/hcpol.2020.26225
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